Fur, Skin, and Ear Mites (Acariasis)
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Introduction to the Arthropods
Ticks General Tick Biology Life cycle has 4 stages: egg, 6-legged larvae, 8-legged nymph, & adult Must consume blood from a host at every stage to develop – each stage must find a new host Pierces skin and attaches to host with mouthparts Feed on mammals, birds, & lizards Larvae & nymphs prefer smaller hosts Life cycle Hard ticks vs Soft ticks Harm to humans Direct injures 1. Irritation: sting, secondary infection, allergy 2. Tick paralysis: paralysis of the motor nerves --- cannot walk or stand, has difficulty in speaking, swallowing and breathing. Transmission of diseases Three medically important tick species American dog tick Blacklegged tick or deer tick Lone star tick. American Dog Tick: Diseases - Carries Rocky Mountain spotted fever - Can also transmit tularemia - Injected dog tick saliva can cause tick paralysis (tick neurotoxin) - Infected tick attached to host 4 – 6 hours before transmitting disease Blacklegged tick or deer tick - Smaller than other ticks - males 1/16”, females ~3/32” - Both sexes are dark chocolate brown, but rear half of adult female is red or orange - Larval stage is nearly translucent - Engorged adult females are brownish Carries Lyme disease May also carry anaplasmosis & ehrlichiosis Can infect a host with two or more diseases simultaneously Infected tick attached to host 36 – 48 hours before disease transmission Lone star tick Adult female is ~3/16” long, brown with distinct silvery spot on upper scutum Male is ~3/16” long, brown with whitish markings along rear edge. Engorged female is almost -
Comparative Study of Mites Infecting Mice and Rats in Al- Diwaniyah City, South of Iraq
Biochem. Cell. Arch. Vol. 18, No. 1, pp. 259-261, 2018 www.connectjournals.com/bca ISSN 0972-5075 COMPARATIVE STUDY OF MITES INFECTING MICE AND RATS IN AL- DIWANIYAH CITY, SOUTH OF IRAQ Habeebwaseelkadhum Shubber and Murtadha Nabeel Murtadha Al-Tameemi Department of Biology, Collage of Science, University of Qadisiyah, Iraq. e-mail : [email protected], [email protected] (Accepted 3 March 2018) ABSTRACT : The study aimed at comparing infection of Myobia musculi with that of Ornithonys susbacoti, during the study period of 2016-2017. A total of 220 rodents were identified including Musmusculus (89), Rattus norvegicus (37), R. rattus (48) & Swiss albino (46). After the specimens are anesthetized, mites are investigated. It was found that Musmusculus were infected byMyobia musculi at 35.9% comparison with Rattus norvegicus, R. rattus and Swiss albino were infected by Ornithonys susbacoti at (29.7%, 41.6%, 8.6%), respectively. Key words : Mits, Myobia musculi, Ornithonys susbacoti, mice, rats. INTRODUCTION Iraq, ectoparasites of wild animals were poorly studied Rodent belong to the Animal kingdom, Chordata (Abul-Hab and Shihab, 1996; Abul-hab, 1984, 1986) phylum- Mammals class within the Real Mammals above reported Ornithonys susbacoti (Hirst, 1913) from the order of above the heading and to the order of Rodentia commensal and semi wild rodents. Then Abul-hab and (Fleer et al, 2011). They are considered the highest orders Shihab (1996) found it on the long-eared hedgehog of Mammals, as they constitute a ration more the 40% Hemiechinus auritus (Gmelin, 1770) collected in Wassit among all kinds of Mammals and the most successful Governorate, Central Iraq. -
2021 Fur Harvester Digest 3 SEASON DATES and BAG LIMITS
2021 Michigan Fur Harvester Digest RAP (Report All Poaching): Call or Text (800) 292-7800 Michigan.gov/Trapping Table of Contents Furbearer Management ...................................................................3 Season Dates and Bag Limits ..........................................................4 License Types and Fees ....................................................................6 License Types and Fees by Age .......................................................6 Purchasing a License .......................................................................6 Apprentice & Youth Hunting .............................................................9 Fur Harvester License .....................................................................10 Kill Tags, Registration, and Incidental Catch .................................11 When and Where to Hunt/Trap ...................................................... 14 Hunting Hours and Zone Boundaries .............................................14 Hunting and Trapping on Public Land ............................................18 Safety Zones, Right-of-Ways, Waterways .......................................20 Hunting and Trapping on Private Land ...........................................20 Equipment and Fur Harvester Rules ............................................. 21 Use of Bait When Hunting and Trapping ........................................21 Hunting with Dogs ...........................................................................21 Equipment Regulations ...................................................................22 -
Plasma Pharmacokinetic Profile of Fluralaner (Bravecto™) and Ivermectin Following Concurrent Administration to Dogs Feli M
Walther et al. Parasites & Vectors (2015) 8:508 DOI 10.1186/s13071-015-1123-8 SHORT REPORT Open Access Plasma pharmacokinetic profile of fluralaner (Bravecto™) and ivermectin following concurrent administration to dogs Feli M. Walther1*, Mark J. Allan2 and Rainer KA Roepke2 Abstract Background: Fluralaner is a novel systemic ectoparasiticide for dogs providing immediate and persistent flea, tick and mite control after a single oral dose. Ivermectin has been used in dogs for heartworm prevention and at off label doses for mite and worm infestations. Ivermectin pharmacokinetics can be influenced by substances affecting the p-glycoprotein transporter, potentially increasing the risk of ivermectin neurotoxicity. This study investigated ivermectin blood plasma pharmacokinetics following concurrent administration with fluralaner. Findings: Ten Beagle dogs each received a single oral administration of either 56 mg fluralaner (Bravecto™), 0.3 mg ivermectin or 56 mg fluralaner plus 0.3 mg ivermectin/kg body weight. Blood plasma samples were collected at multiple post-treatment time points over a 12-week period for fluralaner and ivermectin plasma concentration analysis. Ivermectin blood plasma concentration profile and pharmacokinetic parameters Cmax,tmax,AUC∞ and t½ were similar in dogs administered ivermectin only and in dogs administered ivermectin concurrently with fluralaner, and the same was true for fluralaner pharmacokinetic parameters. Conclusions: Concurrent administration of fluralaner and ivermectin does not alter the pharmacokinetics -
Arthropod Parasites in Domestic Animals
ARTHROPOD PARASITES IN DOMESTIC ANIMALS Abbreviations KINGDOM PHYLUM CLASS ORDER CODE Metazoa Arthropoda Insecta Siphonaptera INS:Sip Mallophaga INS:Mal Anoplura INS:Ano Diptera INS:Dip Arachnida Ixodida ARA:Ixo Mesostigmata ARA:Mes Prostigmata ARA:Pro Astigmata ARA:Ast Crustacea Pentastomata CRU:Pen References Ashford, R.W. & Crewe, W. 2003. The parasites of Homo sapiens: an annotated checklist of the protozoa, helminths and arthropods for which we are home. Taylor & Francis. Taylor, M.A., Coop, R.L. & Wall, R.L. 2007. Veterinary Parasitology. 3rd edition, Blackwell Pub. HOST-PARASITE CHECKLIST Class: MAMMALIA [mammals] Subclass: EUTHERIA [placental mammals] Order: PRIMATES [prosimians and simians] Suborder: SIMIAE [monkeys, apes, man] Family: HOMINIDAE [man] Homo sapiens Linnaeus, 1758 [man] ARA:Ast Sarcoptes bovis, ectoparasite (‘milker’s itch’)(mange mite) ARA:Ast Sarcoptes equi, ectoparasite (‘cavalryman’s itch’)(mange mite) ARA:Ast Sarcoptes scabiei, skin (mange mite) ARA:Ixo Ixodes cornuatus, ectoparasite (scrub tick) ARA:Ixo Ixodes holocyclus, ectoparasite (scrub tick, paralysis tick) ARA:Ixo Ornithodoros gurneyi, ectoparasite (kangaroo tick) ARA:Pro Cheyletiella blakei, ectoparasite (mite) ARA:Pro Cheyletiella parasitivorax, ectoparasite (rabbit fur mite) ARA:Pro Demodex brevis, sebacceous glands (mange mite) ARA:Pro Demodex folliculorum, hair follicles (mange mite) ARA:Pro Trombicula sarcina, ectoparasite (black soil itch mite) INS:Ano Pediculus capitis, ectoparasite (head louse) INS:Ano Pediculus humanus, ectoparasite (body -
MALAYSIAN PARASITIC MITES II. MYOBIIDAE (PROSTIGMATA) from RODENTS L 2 3 A
74 6 Vol. 6,No. 2 Internat. J. Acarol. 109 MALAYSIAN PARASITIC MITES II. MYOBIIDAE (PROSTIGMATA) FROM RODENTS l 2 3 A. Fain , F. S. Lukoschus and M. Nadchatram ----- ABSTRACT-The fur-mites of the family Myobiidae parasitic on rodents in Malaysia are studied. They belong to 9 species and 2 genera Radfordia Ewing and Myobia von Reyden. The new taxa include one new subgenus Radfordia (Rat timyobia); 4 new species~ Radfordia (Rat timyobia) pahangensis, R.(R.) selangorensis, R. (R.) subangensis, Myobia malaysiensis and one new subspecies Radfordia (Radfordia) ensifera jalorensis. These are described and illustrated. In addition, the male of Radfordia (Rat:ttmyouti.a) acinaciseta Wilson, 1967 is described for the first time. ----- During a stay in the Institute for Medical Research, Kuala Lumpur, F. S. L. collected a number of parasitic mites from various hosts (Fain et al., 1980). This paper deals with the species of Myobiidae found on rodents. Nine species in 2 genera-Radfordia and Myobia, , were collected. A new subgenus, Radfordia (Rattimyobia), 4 new species, Radfordia (Rattimyobia) pahangensi s, R. (R.) selangorensis, R. (R.) subangensis, Myobia malaysiensis, and 1 new subspecies, R. (Radfordia ) ensifera jalorensis, are described and illustrated. In addition, the male of R. (Rattimyobia) acinaciseta Wilson is described for the first time. The holotypes are deposited in the British Museum, Natural History, London. Paratypes are in the following institutions: Institute for Medical Research, Kuala Lumpur; Academy of Sciences, Department of Parasitology, Prague; Bernice Bishop Museum, Honolulu; Field Museum of Natural History, Chicago; Institut royal des Sciences naturelles, Bruxelles; Institute of Acaro logy, Columbus; Zoologisches Museum, Hamburg; Rijksmuseum Natural History, Leiden; U. -
Development of a Real-Time Pcr Assay for Mouse Fur Mites
DEVELOPMENT OF A REAL-TIME PCR ASSAY FOR MOUSE FUR MITES AND EVALUATION OF PILOT STUDY by Allison Poore B.S. (Dickinson College) 2012 THESIS Submitted in partial satisfaction of the requirements for the degree of MASTER OF SCIENCE in BIOMEDICAL SCIENCE in the GRADUATE SCHOOL of HOOD COLLEGE May 2019 Accepted: ________________________________ ________________________________ Dr. Craig Laufer, Ph.D. Dr. Ann Boyd, Ph.D. Committee Member Director, Biomedical Science Program ________________________________ ________________________________ Dr. Ann Boyd, Ph.D. Dr. April Boulton, Ph.D. Committee Member Dean of the Graduate School ________________________________ Dr. Wang-Ting Hsieh, Ph.D. Thesis Adviser STATEMENT OF USE AND COPYRIGHT WAIVER I do authorize Hood College to lend this thesis, or reproductions of it, in total or in part, at the request of other institutions or individuals for the purpose of scholarly research. ii DEDICATION To Scott. And to my Mom and Dad. I love you. iii ACKNOWLEDGEMENTS Thank you to the National Cancer Institute for funding and for their continued work to improve the lives of patients living with cancer. Thank you to all the Hood College faculty who have supported me throughout my time as a graduate student. A special thanks to Dr. Ann Boyd, who made every effort to help me finish my degree through every challenge. An additional special thank you to Dr. Rachel Beyer, who also took extra time and provided accommodation to help me finish my classes. Thank you to Dr. Wang-Ting Hsieh for years of mentoring in molecular biology. I am so grateful for the knowledge and experience I have gained as part of your group. -
Laboratory Animal Management: Rodents
THE NATIONAL ACADEMIES PRESS This PDF is available at http://nap.edu/2119 SHARE Rodents (1996) DETAILS 180 pages | 6 x 9 | PAPERBACK ISBN 978-0-309-04936-8 | DOI 10.17226/2119 CONTRIBUTORS GET THIS BOOK Committee on Rodents, Institute of Laboratory Animal Resources, Commission on Life Sciences, National Research Council FIND RELATED TITLES SUGGESTED CITATION National Research Council 1996. Rodents. Washington, DC: The National Academies Press. https://doi.org/10.17226/2119. Visit the National Academies Press at NAP.edu and login or register to get: – Access to free PDF downloads of thousands of scientific reports – 10% off the price of print titles – Email or social media notifications of new titles related to your interests – Special offers and discounts Distribution, posting, or copying of this PDF is strictly prohibited without written permission of the National Academies Press. (Request Permission) Unless otherwise indicated, all materials in this PDF are copyrighted by the National Academy of Sciences. Copyright © National Academy of Sciences. All rights reserved. Rodents i Laboratory Animal Management Rodents Committee on Rodents Institute of Laboratory Animal Resources Commission on Life Sciences National Research Council NATIONAL ACADEMY PRESS Washington, D.C.1996 Copyright National Academy of Sciences. All rights reserved. Rodents ii National Academy Press 2101 Constitution Avenue, N.W. Washington, D.C. 20418 NOTICE: The project that is the subject of this report was approved by the Governing Board of the National Research Council, whose members are drawn from the councils of the National Academy of Sciences, National Academy of Engineering, and Institute of Medicine. The members of the committee responsible for the report were chosen for their special competences and with regard for appropriate balance. -
ESCCAP Guidelines Final
ESCCAP Malvern Hills Science Park, Geraldine Road, Malvern, Worcestershire, WR14 3SZ First Published by ESCCAP 2012 © ESCCAP 2012 All rights reserved This publication is made available subject to the condition that any redistribution or reproduction of part or all of the contents in any form or by any means, electronic, mechanical, photocopying, recording, or otherwise is with the prior written permission of ESCCAP. This publication may only be distributed in the covers in which it is first published unless with the prior written permission of ESCCAP. A catalogue record for this publication is available from the British Library. ISBN: 978-1-907259-40-1 ESCCAP Guideline 3 Control of Ectoparasites in Dogs and Cats Published: December 2015 TABLE OF CONTENTS INTRODUCTION...............................................................................................................................................4 SCOPE..............................................................................................................................................................5 PRESENT SITUATION AND EMERGING THREATS ......................................................................................5 BIOLOGY, DIAGNOSIS AND CONTROL OF ECTOPARASITES ...................................................................6 1. Fleas.............................................................................................................................................................6 2. Ticks ...........................................................................................................................................................10 -
SNF Mobility Model: ICD-10 HCC Crosswalk, V. 3.0.1
The mapping below corresponds to NQF #2634 and NQF #2636. HCC # ICD-10 Code ICD-10 Code Category This is a filter ceThis is a filter cellThis is a filter cell 3 A0101 Typhoid meningitis 3 A0221 Salmonella meningitis 3 A066 Amebic brain abscess 3 A170 Tuberculous meningitis 3 A171 Meningeal tuberculoma 3 A1781 Tuberculoma of brain and spinal cord 3 A1782 Tuberculous meningoencephalitis 3 A1783 Tuberculous neuritis 3 A1789 Other tuberculosis of nervous system 3 A179 Tuberculosis of nervous system, unspecified 3 A203 Plague meningitis 3 A2781 Aseptic meningitis in leptospirosis 3 A3211 Listerial meningitis 3 A3212 Listerial meningoencephalitis 3 A34 Obstetrical tetanus 3 A35 Other tetanus 3 A390 Meningococcal meningitis 3 A3981 Meningococcal encephalitis 3 A4281 Actinomycotic meningitis 3 A4282 Actinomycotic encephalitis 3 A5040 Late congenital neurosyphilis, unspecified 3 A5041 Late congenital syphilitic meningitis 3 A5042 Late congenital syphilitic encephalitis 3 A5043 Late congenital syphilitic polyneuropathy 3 A5044 Late congenital syphilitic optic nerve atrophy 3 A5045 Juvenile general paresis 3 A5049 Other late congenital neurosyphilis 3 A5141 Secondary syphilitic meningitis 3 A5210 Symptomatic neurosyphilis, unspecified 3 A5211 Tabes dorsalis 3 A5212 Other cerebrospinal syphilis 3 A5213 Late syphilitic meningitis 3 A5214 Late syphilitic encephalitis 3 A5215 Late syphilitic neuropathy 3 A5216 Charcot's arthropathy (tabetic) 3 A5217 General paresis 3 A5219 Other symptomatic neurosyphilis 3 A522 Asymptomatic neurosyphilis 3 A523 Neurosyphilis, -
PLENARY SESSION ABSTRACTS Theme: IMMUNITY and AUTOIMMUNITY
PLENARY SESSION ABSTRACTS Theme: IMMUNITY AND AUTOIMMUNITY State-of-the-Art Address Supporting Review What’s new in autoimmune blistering diseases? Epithelial, immune cell and microbial cross- D. F. MURRELL talk in homeostasis and atopic dermatitis Department of Dermatology, St George Hospital, and T. KOBAYASHI UNSW Faculty of Medicine, Sydney, New South Wales, Laboratory for Innate Immune Systems, RIKEN Center Australia for Integrative Medical Sciences (IMS), Yokohama, There are several blistering diseases which occur natu- Japan rally in other species as well as in humans; for example, Skin is a complex and dynamic ecosystem, wherein the pemphigus occurs naturally in dogs and horses and the epithelial cells, immune cells and microbiota engage in inherited blistering disease, epidermolysis bullosa, also active dialogues and maintain barrier integrity and occurs in dogs. Several new validated scoring systems functional immunity. Alterations of the peaceful coexis- to measure the severity of autoimmune blistering dis- tence with the resident microbiota, referred to as dys- ease (AIBD) have been developed which assist in biosis, lead to dysregulation of host immunity. It has demonstrating efficacy of new treatments, such as the been long debated whether the dysbiosis in the skin of Pemphigus Disease Area Index (PDAI) for pemphigus atopic dermatitis is merely a consequence of chronic and Bullous Pemphigoid Disease Area Index (BPDAI) skin inflammation or whether it is actively involved in for pemphigoid. Pemphigus is due to autoantibodies to driving skin inflammation. Microbiome analysis by 16S desmogleins 1 and 3 in human pemphigus foliaceus and rRNA sequencing in humans and dogs with atopic der- vulgaris and desmocollin1 in canine pemphigus foli- matitis showed the shifts in microbial diversity repre- aceus, generated by the late onset activation of the sented by increased proportion of Staphylococcus spp. -
Total Ige As a Serodiagnostic Marker to Aid Murine Fur Mite Detection
Journal of the American Association for Laboratory Animal Science Vol 51, No 2 Copyright 2012 March 2012 by the American Association for Laboratory Animal Science Pages 199–208 Total IgE as a Serodiagnostic Marker to Aid Murine Fur Mite Detection Gordon S Roble,1,2,* William Boteler,5 Elyn Riedel,3 and Neil S Lipman1,4 Mites of 3 genera—Myobia, Myocoptes, and Radfordia—continue to plague laboratory mouse facilities, even with use of stringent biosecurity measures. Mites often spread before diagnosis, predominantly because of detection dif!culty. Current detection methods have suboptimal sensitivity, are time-consuming, and are costly. A sensitive serodiagnostic technique would facilitate detection and ease workload. We evaluated whether total IgE increases could serve as a serodiagnostic marker to identify mite infestations. Variables affecting total IgE levels including infestation duration, sex, age, mite species, soiled-bedding exposure, and ivermectin treatment were investigated in Swiss Webster mice. Strain- and pinworm-associated effects were examined by using C57BL/6 mice and Swiss Webster mice dually infested with Syphacia obvelata and Aspiculuris tetraptera, respectively. Mite infestations led to signi!cant increases in IgE levels within 2 to 4 wk. Total IgE threshold levels and corresponding sensitivity and speci!city values were determined along the continuum of a receiver-operating charac- teristic curve. A threshold of 81 ng/mL was chosen for Swiss Webster mice; values above this point should trigger screening by a secondary, more speci!c method. Sex-associated differences were not signi!cant. Age, strain, and infecting parasite caused variability in IgE responses. Mice exposed to soiled bedding showed a delayed yet signi!cant increase in total IgE.